Visitor Monitoring Drug History: PATANOL
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: PATANOL
FDA Application No: (NDA) 020688
Active Ingredient(s): OLOPATADINE HYDROCHLORIDE
Company: ALCON
 
Label History
 
View the label approved on May 29, 2003 for PATANOL, (NDA) 020688


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/17/2003 016Labeling Revision Letter
Label 
3/13/2002 015Control Supplement  
8/24/2001 014Package Change  
3/16/2001 013Control Supplement  
3/20/2000 012New or Modified Indication Letter 
2/18/2000 011Manufacturing Change or Addition  
8/17/1999 010Control Supplement  
9/28/1999 009Control Supplement  
2/16/1999 008Manufacturing Change or Addition  
2/5/1999 007Manufacturing Change or Addition  
3/11/1999 006Control Supplement  
10/14/1998 005Control Supplement  
8/19/1999 004Package Change  
5/29/1998 003Labeling Revision  
9/4/1998 002Expiration Date Change  
1/15/1998 001Manufacturing Change or Addition  
12/18/1996 000Approval  
 
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